Detailed information for compound 1569052

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 292.37 | Formula: C17H24O4
  • H donors: 1 H acceptors: 2 LogP: 3.3 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCCCCC(CC(=O)CCc1ccc2c(c1)OCO2)O
  • InChi: 1S/C17H24O4/c1-2-3-4-5-14(18)11-15(19)8-6-13-7-9-16-17(10-13)21-12-20-16/h7,9-10,14,18H,2-6,8,11-12H2,1H3
  • InChiKey: NPZZCENHZLRAHT-UHFFFAOYSA-N  

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

No curated genes were found associated with this compound

Predicted pathogen targets for this compound

By orthology
No druggable targets predicted by orthology data
By sequence similarity to non orthologous known druggable targets
No druggable targets predicted by sequence similarity

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Onchocerca volvulus 0.0077 0.3351 1
Loa Loa (eye worm) DOMON domain-containing protein 0.0077 0.3351 1
Echinococcus multilocularis ankyrin repeat protein 0.0192 0.9765 0.9742
Leishmania major hypothetical protein, conserved 0.0034 0.092 0.5
Brugia malayi Muscle positioning protein 4 0.0077 0.3351 1
Schistosoma mansoni hypothetical protein 0.0077 0.3351 0.3431
Schistosoma mansoni hypothetical protein 0.0034 0.092 0.0942
Toxoplasma gondii kringle domain-containing protein 0.0034 0.092 0.5
Trypanosoma cruzi hypothetical protein, conserved 0.0034 0.092 0.5
Loa Loa (eye worm) hypothetical protein 0.0077 0.3351 1
Loa Loa (eye worm) hypothetical protein 0.0077 0.3351 1
Onchocerca volvulus 0.0077 0.3351 1
Plasmodium vivax cysteine repeat modular protein 1, putative 0.0034 0.092 0.5
Echinococcus granulosus transient receptor potential cation channel 0.0196 0.9984 1
Onchocerca volvulus 0.0077 0.3351 1
Plasmodium falciparum cysteine repeat modular protein 1 0.0034 0.092 0.5
Brugia malayi SEA domain containing protein 0.0077 0.3351 1
Echinococcus granulosus ankyrin repeat protein 0.0192 0.9765 0.9759
Schistosoma mansoni transient receptor potential cation channel subfamily A member 0.0192 0.9765 1
Onchocerca volvulus 0.0077 0.3351 1
Schistosoma mansoni subfamily S1A unassigned peptidase (S01 family) 0.0025 0.0414 0.0424
Onchocerca volvulus 0.0077 0.3351 1

Activities

Activity type Activity value Assay description Source Reference
Efficacy (functional) < 10 % Agonist activity at rat TRPA1 ion channel expressed in HEK293 cells assessed as calcium influx by fluo-4-Am-based fluorimetry relative to allyl isothiocyanate ChEMBL. 22257892
Efficacy (functional) < 10 % Agonist activity at human TRPV1 ion channel expressed in HEK293 cells assessed as calcium influx by fluo-4-Am-based fluorimetry relative to ionomycin ChEMBL. 22257892
IC50 (functional) > 100 uM Antagonist activity at human TRPV1 ion channel expressed in HEK293 cells assessed as inhibition of capsaicin-induced calcium influx incubated for 5 mins prior to capsicin-induction by fluo-4-AM-based fluorimetry ChEMBL. 22257892
IC50 (functional) > 100 uM Antagonist activity at rat TRPA1 ion channel expressed in HEK293 cells assessed as inhibition of AITC-induced calcium influx incubated for 5 mins prior to AITC-induction by fluo-4-AM-based fluorimetry ChEMBL. 22257892

Phenotypes

Whole-cell/tissue/organism interactions

We have no records of whole-cell/tissue assays done with this compound What does this mean?

Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.

Annotated phenotypes:

We have no manually annotated phenotypes for this drug. What does this mean? / Care to help?
In TDR Targets, information about phenotypes that are caused by drugs, or by genetic manipulation of cells (e.g. gene knockouts or knockdowns) is manually curated from the literature. These descriptions help to describe the potential of the target for drug development. If no information is available for this gene or if the information is incomplete, this may mean that i) the papers containing this information either appeared after the curation effort for this organism was carried out or they were inadvertently missed by curators; or that ii) the curation effort for this organism has not yet started.
 
In any case, if you have information about papers containing relevant validation data for this target, please log in using your TDR Targets username and password and send them to us using the corresponding form in this page (only visible to registered users) or contact us.

External resources for this compound

Bibliographic References

1 literature reference was collected for this gene.

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